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Clinical Trials Advisor (CTA) is designed especially for the clinical trials professional charged with gathering submission-quality data while protecting the safety and welfare of study subjects.

With 12 issues a year, you can be confident that you'll stay abreast of the latest developments in global clinical trial trends, changes in trial endpoints and regulations that govern drug and medical device clinical trials.

Each issue of Clinical Trials Advisor provides:

  • Essential industry news, including international news, to keep you fully compliant
  • Tested techniques to keep your clinical trials safe, compliant and efficient

Your subscription also includes access to The Clinical Trials Advisor Regulatory Resource Center — a one-stop location for all the guidance, regulation and laws you’ll need to comply with U.S and international clinical trial requirements. The resource center is updated continuously and available to you around the clock.


Monthly, 12 issues/year. Electronic delivery.

 
 

$745 $445

 

Bonus

Renew Clinical Trials Advisor NOW and receive a FREE copy of our webinar, Reporting Failed Trial Data: New Rules for ClinicalTrials.gov — a $287 value.  Also receive a FREE copy of our management report, Implementing e-Consent for Clinical Trials — a $397 value!

Key Benefits

LINKS TO KEY DOCUMENTS — Need to read regulatory references, guidances, enforcement actions, and other documents? Simply click on the source documents in your electronic issue.

ONLINE ACCESS — Consider our newsletter archive your personal library! Search your current issue — and hundreds of past issues — by keyword and relevancy.